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Author/Creator Falik Zaccai, Tzipora C.

1. A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Issue 4 (April 2022)

Authors:
Issler, Naomi; Afonso, Sara; Weissman, Irith; Jordan, Katrin; Cebrian-Serrano, Alberto; Meindl, Katrin; Dahlke, Eileen; Tziridis, Konstantin; Yan, Guanhua; Robles-López, José M.; Tabernero, Lydia; Patel, Vaksha; Kesselheim, Anne; Klootwijk, Enriko D.; Stanescu, Horia C.; Dumitriu, Simona; Iancu, ...
Journal:
Journal of the American Society of Nephrology
Issue:
Volume 33:Issue 4(2022)
Page Start:
732
Record Type:
Journal Article
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2. Localized Provoked Vulvodynia: Association With Nerve Growth Factor and Transient Receptor Potential Vanilloid Type 1 Genes Polymorphisms. Issue 1 (January 2019)

Authors:
Kalfon, Limor; Azran, Audrey; Farajun, Yaniv; Golan-Hamu, Oshrat; Toben, Aylah; Abramov, Liora; Yeshaya, Arie; Yakir, Orly; Zarfati, Doron; Falik Zaccai, Tzipora C.; Bornstein, Jacob
Journal:
Journal of lower genital tract disease
Issue:
Volume 23:Issue 1(2019:Jan.)
Page Start:
Record Type:
Journal Article
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3. Two novel mutations identified in familial cases with Donohue syndrome. Issue 1 (14th November 2013)

Authors:
Falik Zaccai, Tzipora C.; Kalfon, Limor; Klar, Aharon; Elisha, Mordechai Ben; Hurvitz, Haggit; Weingarten, Galina; Chechik, Emelia; Fleisher Sheffer, Vered; Haj Yahya, Raid; Meidan, Gal; Gross‐Kieselstein, Eva; Bauman, Dvora; Hershkovitz, Sylvia; Yaron, Yuval; Orr‐Urtreger, Avi; Wertheimer, Efrat
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 2:Issue 1(2014:Jan.)
Page Start:
64
Record Type:
Journal Article
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